Canonical Allele Identifier: CA466159195
Gene: CCDC180 HGNC NCBI
SUGT1P4-STRA6LP-CCDC180 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.100105798A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97343516A>C , CM000671.2:g.97343516A>C GRCh38
NC_000009.11:g.100105798A>C , CM000671.1:g.100105798A>C GRCh37
NC_000009.10:g.99145619A>C NCBI36
NG_052792.1:g.41213A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000529487.3:c.2451A>C (CCDC180) MANE Select ENSP00000434727.2:p.Ile817=
ENST00000460482.6:n.2785A>C (CCDC180)
ENST00000494917.6:n.2654A>C (CCDC180)
ENST00000528678.1:n.547A>C (CCDC180)
ENST00000529487.1:c.2583A>C (CCDC180) ENSP00000434727.1:p.Ile861=
ENST00000530011.1:n.236-5595A>C (CCDC180)
NM_020893.2:c.2583A>C (CCDC180) NP_065944.2:p.Ile861=
NR_036527.1:n.4006A>C (SUGT1P4-STRA6LP-CCDC180)
NR_036528.1:n.4006A>C (SUGT1P4-STRA6LP-CCDC180)
NR_036529.1:n.3566A>C (SUGT1P4-STRA6LP-CCDC180)
NM_001348010.1:c.2574A>C (CCDC180) NP_001334939.1:p.Ile858=
NM_020893.3:c.2583A>C (CCDC180) NP_065944.2:p.Ile861=
NM_001348010.2:c.2574A>C (CCDC180) NP_001334939.1:p.Ile858=
NM_020893.4:c.2583A>C (CCDC180) NP_065944.2:p.Ile861=
NM_001348010.4:c.2442A>C (CCDC180) NP_001334939.2:p.Ile814=
NM_020893.6:c.2451A>C (CCDC180) MANE Select NP_065944.3:p.Ile817=